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Discontinuous microduplications at chromosome 10q24.31 identified in a Chinese family with split hand and foot malformation
BACKGROUND: Split hand/foot malformation (SHFM) is a congenital disorder characterized by a cleft of the hands and/or feet due to dificiency of central rays. Genomic rearrangement at 10q24 has been found to cause nonsyndromic SHFM (SHFM3). METHODS: Four patients and fourteen unaffected individuals f...
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| Hauptverfasser: | , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2013
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3637097/ https://ncbi.nlm.nih.gov/pubmed/23596994 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-14-45 |
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